CAS: 55750-53-3; 6-Maleimidohexanoic Acid

相似化合物

57079-01-3 90267-85-9 57078-99-6

上下游产品

CAS号57079-14-8 (Z)-6-(3-羧基丙烯酰胺)己酸 | CAS号108-31-6 顺酐 | CAS号60-32-2 6-氨基己酸 | CAS号7440-44-0 活性炭 | CAS号55750-63-5 6-(马来酰亚胺基)己酸琥珀酰亚胺酯 | CAS号57-13-6 尿素 | CAS号157503-18-9 1-(6-羟基己基)-1H-吡... | CAS号82333-93-5 hexanoyl chlori...

6-氨基己酸置于溶剂黄146体系中,化学反应 4.0H,反应生成 6-马来酰亚胺基己酸
参考文献:一种新的含巯基多肽的聚乙二醇化试剂的制备
标题:一种新的含巯基多肽的聚乙二醇化试剂的制备
摘要:在dcc等存在下,制备peg的n-马来酰亚胺基-6-氨基己酰基酯,作为取代mal-Sac-Peg的新的巯基-Peg化试剂.
DOI:10.1016/s0040-4039(00)78260-8

专利信息

专利号:US-2019292310-A1
优先权日:2018-03-20
标 题:Synthesis of high density molecular dna brushes via organic-phase ring-opening metathesis (co)polymerization
发明人：ZHANG KE; TAN XUYU
权利人:UNIV NORTHEASTERN
摘要:The invention provides novel synthetic methods for oligonucleotide polymerization reactions that separate the deprotection and cleavage step following solid-phase oligonucleotide synthesis into two separate steps, thereby providing fully protected hydrophobic oligonucleotides that can be further manipulated in organic solvents. The disclosed methods enable the synthesis of new structures, such as brush DNA and brush RNA polymers and micellar spherical nucleic acids (SNAs

专利号:US-6262251-B1
优先权日:1995-10-19
标题 :Method for solution phase synthesis of oligonucleotides
发明人：PIEKEN WOLFGANG; MCGEE DANNY; SETTLE ALECIA; ZHAI YANSHENG; HUANG JIANPING
权利人:PROLIGO LLC
摘要:This invention discloses an improved method for the sequential solution phase synthesis of oligonucleotides. The method lends itself to automation and is ideally suited for large scale manufacture of oligonucleotides with high efficiency.

专利号:US-4670563-A
优先权日:1984-06-20
标题 :Imidazolides as intermediates for the synthesis of cytotoxic conjugates
发明人：JANSEN FRANZ; GROS PIERRE
权利人:SANOFI SA
摘要:Imidazolides of the formula: ##STR1## in which: E represents an inert spacing structure; and n G represents a group: ##STR2## or a group --S--S--X, in which X is an activating group. Application: synthesis of cytotoxic conjugates.

专利号:WO-9847910-A1
优先权日:1997-04-21
标题:Method for solution phase synthesis of oligonucleotides
发明人：PIEKEN WOLFGANG; MCGEE DANNY; SETTLE ALECIA; ZHAI YANSHENG; HUANG JIANPING; HILL KEN; SMITH RANDALL S
权利人:NEXSTAR PHARMACEUTICALS INC; PIEKEN WOLFGANG; MCGEE DANNY; SETTLE ALECIA; ZHAI YANSHENG; HUANG JIANPING; HILL KEN; SMITH RANDALL S
摘要:This invention discloses an improved method for the sequential solution phase synthesis of oligonucleotides. The method lends itself to automation and is ideally suited for large scale manufacture oligonucleotides with high efficiency.

专利号:US-5874532-A
优先权日:1997-01-08
标 题 :Method for solution phase synthesis of oligonucleotides and peptides
发明人：PIEKEN WOLFGANG; GOLD LARRY
权利人:NEXSTAR PHARMACEUTICALS INC
摘要:This invention discloses an improved method for the sequential solution phase synthesis of oligonucleotides and peptides. The method lends itself to automation and is ideally suited for large scale manufacture oligonucleotides with high efficiency.

专利号:US-6001966-A
优先权日:1995-10-19
标题 :Method for solution phase synthesis of oligonucleotides and peptides
发明人：PIEKEN WOLFGANG; GOLD LARRY
权利人:PROLIGO LLC
摘要:This invention discloses an improved method for the sequential solution phase synthesis of oligonucleotides and peptides. The method lends itself to automation and is ideally suited for large scale manufacture oligonucleotides with high efficiency.